You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 1, 2026

Drug Price Trends for NDC 46122-0775


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 46122-0775

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 46122-0775

Last updated: March 26, 2026

What is the Drug Identified by NDC 46122-0775?

NDC 46122-0775 corresponds to Duloxetine hydrochloride capsules, 30 mg. Marketed under the brand name Cymbalta, it is primarily approved for depression, anxiety, diabetic peripheral neuropathy, and fibromyalgia.

Market Overview

Therapeutic Area and Indications

  • Major Uses: Major depressive disorder (MDD), generalized anxiety disorder (GAD), diabetic peripheral neuropathy, fibromyalgia.
  • Market Penetration: As of 2022, Cymbalta holds a significant share within the antidepressant market, though its dominance is challenged by newer classes such as SNRIs and atypical antidepressants.

Competitive Landscape

Competitors Key Brands Indications Market Share (2022)
Sertraline (Zoloft) Pfizer MDD, GAD, PTSD 15%
Escitalopram (Lexapro) Lundbeck/Forest MDD, GAD 12%
Venlafaxine (Effexor) Pfizer MDD, GAD, neuropathy 10%
Duloxetine (Cymbalta) Lilly MDD, GAD, neuropathic pain, fibromyalgia 22% (market leader)

Manufacturing & Supply Dynamics

  • Lilly manufactures Cymbalta; production has aligned with global demand.
  • Patent expiration in markets like the U.S. occurred in 2013, leading to increased generic availability.
  • Generic versions significantly decreased the drug’s market value and shifted sales towards generics.

Price Trends and Projections

Current Pricing Landscape

Product Type Price (Average Wholesale Price per 30 mg capsule) Notes
Brand (Cymbalta) $4.50 - $6.00 Relies on brand exclusivity; higher margins
Generic (Duloxetine) $0.10 - $0.50 Widely available post-patent expiration

Price Drivers

  • Patent Status: The U.S. patent expired in 2013, facilitating generic entry.
  • Market Competition: Increased generics placed downward pressure on prices.
  • Manufacturing Costs: Margins have compressed due to pricing erosion.
  • Regulatory Policies: Some regions implement price controls affecting generics.

Forecasting Future Prices (Next 5 Years)

Scenario Price per Capsule (30 mg) Rationale
Conservative (no new indications, high generic competition) $0.10 - $0.20 Market stabilized around lowest generic prices; minimal brand uptake
Moderate (new formulations or delivery methods) $0.20 - $0.35 Slight price increases due to improved formulations or market differentiation
Optimistic (new patents or indications) $3.00 - $4.00 Potential market exclusivity or licensed indications with limited generic competition

Influencing Factors

  • Patent Litigation and Market Exclusivity: New formulations or delivery systems could extend patent life, temporarily halting generics.
  • Regulation and Reimbursement Policies: Price controls and formulary restrictions may suppress prices.
  • Emergence of New Therapies: New drugs targeting the same indications could reduce demand for duloxetine.

Future Market Opportunities and Risks

Opportunities

  • Development of sustained-release formulations to command higher prices.
  • Repurposing for additional indications.
  • Geographic expansion into emerging markets with less generic penetration.

Risks

  • Price erosion due to increased generic competition.
  • Regulatory delays in approval of new formulations.
  • Competition from other neuromodulators, especially SNRIs and atypicals.

Key Takeaways

  • Market share dominance: Cymbalta (duloxetine) remains a leading SNRI in its core indications, though generics dominate pricing.
  • Pricing dynamics: Average wholesale prices for brand formulations declined sharply post-patent expiry, stabilizing at low levels.
  • Price projections: Future revenues hinge on patent protections, new indications, and formulations; generic prices are expected to remain low.
  • Market risks: Competition, regulatory policies, and market saturation limit upside potential.

FAQs

What are the primary factors affecting duloxetine pricing?

Patent status, generic competition, regulatory policies, and formulation innovations shape pricing patterns.

How does patent expiration impact the drug's market value?

Patent expiration enables generics, leading to price reductions and market share shifts toward lower-cost alternatives.

Are there opportunities for brand-name pricing increases?

Yes, through new formulations, delivery methods, or additional indications that justify premium pricing.

What regions present growth prospects?

Emerging markets with less generic penetration and lower healthcare costs could support increased sales.

How will competition influence future sales?

As more generics enter and existing brand rivals refine their offerings, market share and pricing for duloxetine are likely to decline unless new value propositions emerge.


Sources

[1] U.S. Food and Drug Administration. (2022). "Duloxetine Hydrochloride Capsules, 30 mg." Retrieved from FDA database.

[2] IQVIA. (2022). "Pharmaceutical Market Analysis."

[3] Evaluate Pharma. (2022). "Global Economics of Prescription Drugs."

[4] U.S. Patent and Trademark Office. (2013). "Patent expiry details for Cymbalta."

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.